About this role
Clinical Research Safety Associate at Everest Clinical Research. Location: Markham or Bridgewater or Shanghai or Taipei or Canada. Role: serving DMC, performing QC, writing documents Requirements: MSc or PhD in a clinical/medical/health field, 2+ years clinical research experience in academic/pharma/CRO, Phase I-IV trial knowledge, experience with clinical data systems preferred, strong writing and MS Office skills. Category: Research and Development (R&D) Seniority: Entry Level Tools: Microsoft Office Commitment: Full Time Workplace: Hybrid Languages: English